2VSZ

Crystal Structure of the ELMO1 PH domain

2VSZ の概要

• エントリーDOI: 10.2210/pdb2vsz/pdb
• 分子名称: ENGULFMENT AND CELL MOTILITY PROTEIN 1 (2 entities in total)
• 機能のキーワード: apoptosis, rac signalling, sh3-binding, phagocytosis, elmo, dock180, phosphoinositide binding, guanine nucleotide exchange factor
• 由来する生物種: HOMO SAPIENS (HUMAN)
• 細胞内の位置: Cytoplasm: Q92556
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 34205.50

構造登録者

Komander, D.,Patel, M.,Barford, D.,Cote, J.-F. (登録日: 2008-05-01, 公開日: 2009-03-10, 最終更新日: 2024-05-08)

主引用文献

Komander, D.,Patel, M.,Laurin, M.,Fradet, N.,Pelletier, A.,Barford, D.,Cote, J.-F.
An Alpha-Helical Extension of the Elmo1 Pleckstrin Homology Domain Mediates Direct Interaction to Dock180 and is Critical in Rac Signaling.
Molecular Biology of the Cell, 19:4837-, 2008

PubMed Abstract: The mammalian DOCK180 protein belongs to an evolutionarily conserved protein family, which together with ELMO proteins, is essential for activation of Rac GTPase-dependent biological processes. Here, we have analyzed the DOCK180-ELMO1 interaction, and map direct interaction interfaces to the N-terminal 200 amino acids of DOCK180, and to the C-terminal 200 amino acids of ELMO1, comprising the ELMO1 PH domain. Structural and biochemical analysis of this PH domain reveals that it is incapable of phospholipid binding, but instead structurally resembles FERM domains. Moreover, the structure revealed an N-terminal amphiphatic alpha-helix, and point mutants of invariant hydrophobic residues in this helix disrupt ELMO1-DOCK180 complex formation. A secondary interaction between ELMO1 and DOCK180 is conferred by the DOCK180 SH3 domain and proline-rich motifs at the ELMO1 C-terminus. Mutation of both DOCK180-interaction sites on ELMO1 is required to disrupt the DOCK180-ELMO1 complex. Significantly, although this does not affect DOCK180 GEF activity toward Rac in vivo, Rac signaling is impaired, implying additional roles for ELMO in mediating intracellular Rac signaling.

PubMed: 18768751
DOI: 10.1091/MBC.E08-04-0345

実験手法

X-RAY DIFFRACTION (2.3 Å)